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Acetyl Hexapeptide 3

Argireline, Acetyl Hexapeptide-8

Quick Stats
Studies 21
Trials 6
Score 4
2025 pubmed 1 citations

Development of a Sensory Neuron-Integrated Skin Spheroid Model for the Evaluation of Neuropeptide-Based Topical Delivery Systems.

Martin. Bianca Aparecida BA; Viegas. Juliana J; Dalmolin. Luciana Facco LF; Santos. Emerson de Souza ES; Vatanabe. Izabela Pereira IP; Lisboa. Sabrina Francesca SF; Lopez. Renata Fonseca Vianna RFV; Sarmento. Bruno B

Key Findings

  • Acetyl‑hexapeptide‑3 penetrates the stratum corneum and accumulates near sensory neurons in a skin spheroid model and in real human skin.
  • Topical HEX‑3 reduces acetylcholine release, boosts the antioxidant enzyme SOD2, and increases type I collagen production, especially in aged skin.
  • Treatment improves skin hydration, lessens scaling, and restores the structural organization of the outer skin layer within 48 hours.

Practical Outcomes

  • For DIY skin‑care enthusiasts, this study supports using topical acetyl‑hexapeptide‑3 as an anti‑aging ingredient that can enhance collagen, improve hydration, and provide antioxidant benefits. While the exact dose isn’t specified, formulations that allow the peptide to reach deeper skin layers (e.g., using penetration‑enhancing carriers or film patches) are likely to be most effective.

Summary

Researchers built a tiny 3‑D skin model that includes nerve cells and showed that a peptide called acetyl‑hexapeptide‑3 (often sold as Argireline) can get through the outer skin layer, gather around the nerves, and trigger several skin‑health benefits.

Abstract

The skin is a complex organ composed of multiple layers and diverse cell types, including keratinocytes, fibroblasts, adipocytes, and sensory neurons, which maintain its structural and functional integrity together. Conventional in vitro and ex vivo models help investigate drug permeation and selected biological effects. However, they are limited in replicating neural interactions critical for assessing the efficacy of neuropeptide-based therapies. To address this limitation, a sensory neuron-integrated skin spheroid (SS) model was established, incorporating key skin cell types and providing a rapid, adaptable, and physiologically relevant platform for screening the biological activity of topical delivery systems targeting neuronal pathways. The model's responsiveness was demonstrated using acetyl hexapeptide-3 (HEX-3), a neuropeptide that inhibits acetylcholine release. HEX-3 was internalized by spheroid cells, with preferential accumulation around sensory neurons, confirming targeted cellular uptake. In parallel, ex vivo human skin studies confirmed that HEX-3 can traverse the stratum corneum and accumulate in deeper layers. Treatment with this film enhanced skin hydration, reduced scaling, and improved the structural organization of the stratum corneum after 48 h. Functional assays using the SS model showed that HEX-3 treatment suppressed acetylcholine release, upregulated the antioxidant enzyme SOD2, and stimulated type I collagen synthesis. In aged skin samples, the application of HEX-3 significantly increased collagen levels. This effect was mirrored in the spheroid model, which reached collagen levels comparable to those of aged human skin upon treatment. These findings establish the SS model as a robust platform for evaluating the biological activity of neuropeptide-based topical therapies, offering valuable insights for developing advanced strategies for skin rejuvenation and repair.

Study Information

Provider

pubmed

Year

2025

Date

2025-05-23T00:00:00.000Z

DOI

10.1021/acsbiomaterials.5c00141

Citations

1

References

64